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NDC 61919-0628-90 IBUPROFEN 600 mg/1 Details
IBUPROFEN 600 mg/1
IBUPROFEN is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Direct_Rx. The primary component is IBUPROFEN.
Product Information
| NDC | 61919-0628 |
|---|---|
| Product ID | 61919-628_fb47e2b8-5e53-72ad-e053-6394a90afcbb |
| Associated GPIs | 66100020000330 |
| GCN Sequence Number | 008349 |
| GCN Sequence Number Description | ibuprofen TABLET 600 MG ORAL |
| HIC3 | S2B |
| HIC3 Description | NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS |
| GCN | 35742 |
| HICL Sequence Number | 003723 |
| HICL Sequence Number Description | IBUPROFEN |
| Brand/Generic | Generic |
| Proprietary Name | IBUPROFEN |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | IBUPROFEN |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 600 |
| Active Ingredient Units | mg/1 |
| Substance Name | IBUPROFEN |
| Labeler Name | Direct_Rx |
| Pharmaceutical Class | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA091625 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 61919-0628-90 (61919062890)
| NDC Package Code | 61919-628-90 |
|---|---|
| Billing NDC | 61919062890 |
| Package | 90 TABLET, FILM COATED in 1 BOTTLE (61919-628-90) |
| Marketing Start Date | 2019-08-20 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |